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本文引用的文献

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Genetic variations affecting serum carcinoembryonic antigen levels and status of regional lymph nodes in patients with sporadic colorectal cancer from Southern China.影响中国南方散发性结直肠癌患者血清癌胚抗原水平及区域淋巴结状态的基因变异
PLoS One. 2014 Jun 18;9(6):e97923. doi: 10.1371/journal.pone.0097923. eCollection 2014.
2
Fucosyltransferase 2: a genetic risk factor for primary sclerosing cholangitis and Crohn's disease--a comprehensive review.岩藻糖基转移酶 2:原发性硬化性胆管炎和克罗恩病的遗传风险因素——全面综述。
Clin Rev Allergy Immunol. 2015 Jun;48(2-3):182-91. doi: 10.1007/s12016-014-8423-1.
3
Fut2 genotype is a risk factor for dominant stenosis and biliary candida infections in primary sclerosing cholangitis.Fut2 基因型是原发性硬化性胆管炎中显性狭窄和胆道念珠菌感染的危险因素。
Aliment Pharmacol Ther. 2014 Apr;39(8):873-82. doi: 10.1111/apt.12663. Epub 2014 Feb 24.
4
FUT2 and FUT3 genotype determines CA19-9 cut-off values for detection of cholangiocarcinoma in patients with primary sclerosing cholangitis.FUT2 和 FUT3 基因型决定原发性硬化性胆管炎患者中用于胆管癌检测的 CA19-9 截断值。
J Hepatol. 2013 Dec;59(6):1278-84. doi: 10.1016/j.jhep.2013.08.005. Epub 2013 Aug 16.
5
A genome wide association study of genetic loci that influence tumour biomarkers cancer antigen 19-9, carcinoembryonic antigen and α fetoprotein and their associations with cancer risk.一项全基因组关联研究,旨在发现影响肿瘤标志物癌抗原 19-9、癌胚抗原和甲胎蛋白的遗传位点,及其与癌症风险的关联。
Gut. 2014 Jan;63(1):143-51. doi: 10.1136/gutjnl-2012-303434. Epub 2013 Jan 7.
6
Primary sclerosing cholangitis: new approaches to diagnosis, surveillance and treatment.原发性硬化性胆管炎:诊断、监测和治疗的新方法。
Dig Dis. 2012;30 Suppl 1:39-47. doi: 10.1159/000341123. Epub 2012 Oct 11.
7
Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci.原发性硬化性胆管炎全基因组关联研究的扩展分析检测到多个新的风险位点。
J Hepatol. 2012 Aug;57(2):366-75. doi: 10.1016/j.jhep.2012.03.031. Epub 2012 Apr 18.
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Primary sclerosing cholangitis: diagnostic and therapeutic problems.原发性硬化性胆管炎:诊断和治疗问题。
Dig Dis. 2011;29 Suppl 1:41-5. doi: 10.1159/000331074. Epub 2011 Nov 15.
9
Endoscopic dilation of dominant stenoses in primary sclerosing cholangitis: outcome after long-term treatment.原发性硬化性胆管炎中优势狭窄的内镜扩张:长期治疗后的结果。
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Diagnosis and management of primary sclerosing cholangitis.原发性硬化性胆管炎的诊断与管理
Hepatology. 2010 Feb;51(2):660-78. doi: 10.1002/hep.23294.

常见的岩藻糖基转移酶 2 基因变异与血清癌胚抗原水平相关,并影响原发性硬化性胆管炎患者的癌症筛查。

A common genetic variant of fucosyltransferase 2 correlates with serum carcinoembryonic antigen levels and affects cancer screening in patients with primary sclerosing cholangitis.

机构信息

Department of Internal Medicine IV, University Hospital Heidelberg, Heidelberg, Germany.

Norwegian PSC Research Center, Division of Cancer Medicine, Surgery and Transplantation, Oslo University Hospital, Rikshospitalet, Oslo, Norway.

出版信息

United European Gastroenterol J. 2016 Feb;4(1):84-91. doi: 10.1177/2050640615581577. Epub 2015 Apr 9.

DOI:10.1177/2050640615581577
PMID:26966527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4766541/
Abstract

BACKGROUND

Primary sclerosing cholangitis (PSC) patients are at increased risk of biliary tract cancer, and carcinoembryonic antigen (CEA) serum levels might be used for screening.

OBJECTIVE

To examine cancer screening with CEA in PSC patients and analyse how serum CEA levels are affected by genetic variants of fucosyltransferase (FUT) 2 and 3.

METHODS

In a retrospective cohort analysis we evaluated CEA levels in 226 PSC patients, including 19 with biliary malignancy, and investigated how FUT2 and FUT3 SNPs affected CEA levels. Receiver-operating-characteristic (ROC) analysis was performed and cut-off values were determined based on Youden's index. A control cohort contained 240 patients, including 28 with biliary malignancy.

RESULTS

Median CEA concentration was lower in cancer-free patients (1.4 ng/mL) than in cancer patients (2.0 ng/mL, P = 0.014). ROC analysis revealed an area under the curve (AUC) of 0.671, the optimal cut-off was 3.2 ng/mL. The FUT2 variant rs601338 (G428A) correlated with CEA levels, and the effect was most prominent in a subgroup of patients genetically incapable of expressing CA19-9. The AUC improved if ROC analysis was performed separately for wild-type (AUC: 0.731) and homozygous mutant (AUC: 0.816) G428A. The influence of FUT2 on CEA was confirmed in the control cohort.

CONCLUSIONS

CEA is interesting for biliary-malignancy screening in PSC patients, especially in patients who do not express CA19-9. This is the first study to show that the combined use of CEA measurement and FUT genotyping is clinically beneficial and that it might enhance the early detection of biliary malignancy in clinical practice. This approach could also be effective when screening for other common gastrointestinal malignancies.

摘要

背景

原发性硬化性胆管炎(PSC)患者发生胆道癌的风险增加,癌胚抗原(CEA)血清水平可用于筛查。

目的

研究 CEA 在 PSC 患者中的筛查作用,并分析血清 CEA 水平如何受岩藻糖转移酶(FUT)2 和 3 基因变异的影响。

方法

在回顾性队列分析中,我们评估了 226 例 PSC 患者的 CEA 水平,其中 19 例患有胆道恶性肿瘤,并研究了 FUT2 和 FUT3 SNP 如何影响 CEA 水平。进行了受试者工作特征(ROC)分析,并根据 Youden 指数确定了截断值。对照队列包含 240 例患者,其中 28 例患有胆道恶性肿瘤。

结果

无癌症患者的 CEA 浓度中位数(1.4ng/mL)低于癌症患者(2.0ng/mL,P=0.014)。ROC 分析显示曲线下面积(AUC)为 0.671,最佳截断值为 3.2ng/mL。FUT2 变异 rs601338(G428A)与 CEA 水平相关,其影响在不能表达 CA19-9 的患者亚组中最为明显。如果分别对野生型(AUC:0.731)和纯合突变型(AUC:0.816)G428A 进行 ROC 分析,AUC 会提高。在对照队列中也证实了 FUT2 对 CEA 的影响。

结论

CEA 对 PSC 患者的胆道恶性肿瘤筛查很有意义,尤其是不表达 CA19-9 的患者。这是第一项表明联合使用 CEA 测量和 FUT 基因分型具有临床益处并可能增强临床实践中胆道恶性肿瘤早期检测的研究。这种方法在筛查其他常见胃肠道恶性肿瘤时也可能有效。